Canonical Allele Identifier: CA7659948
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs752546701
ExAC: 15:75044201 T / A
gnomAD v4: 15-74751860-T-A
MyVariant Identifiers: chr15:g.75044201T>A (hg19) chr15:g.75044201_75044202delinsAG (hg19) chr15:g.74751860T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74751860T>A , CM000677.2:g.74751860T>A GRCh38
NC_000015.9:g.75044201T>A , CM000677.1:g.75044201T>A GRCh37
NC_000015.8:g.72831254T>A NCBI36
NG_008431.1:g.34319T>A
NG_008431.2:g.34319T>A
NG_061543.1:g.8016T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1042+6T>A MANE Select ENSP00000342007.4:n.1042+6T>A
ENST00000343932.4:c.1042+6T>A ENSP00000342007.4:n.1042+6T>A
NM_000761.4:c.1042+6T>A NP_000752.2:n.1042+6T>A
NM_000761.5:c.1042+6T>A MANE Select NP_000752.2:n.1042+6T>A
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